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rs72558462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558462(A;T)
Make rs72558462(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411897
GeneOTC
is asnp
is mentioned by
dbSNPrs72558462
ebirs72558462
HLIrs72558462
Exacrs72558462
Varsomers72558462
Maprs72558462
PheGenIrs72558462
hapmaprs72558462
1000 genomesrs72558462
hgdprs72558462
ensemblrs72558462
gopubmedrs72558462
geneviewrs72558462
scholarrs72558462
googlers72558462
pharmgkbrs72558462
gwascentralrs72558462
openSNPrs72558462
23andMers72558462
23andMe allrs72558462
SNP Nexus

SNPshotrs72558462
SNPdbers72558462
MSV3drs72558462
GWAS Ctlgrs72558462
Max Magnitude0
ClinVar
Risk rs72558462(T;T)
Alt rs72558462(T;T)
Reference rs72558462(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271150A>T
CLNSRC ClinVar
CLNACC RCV000083598.1,